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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967342Generated: October 30, 2026

Methanol → HCID 91513383, compound

https://huagongshe.com/reaction/967342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantSodium hydrideHCID 24758—
ReactantHCID 91272540HCID 91272540—
SolventDimethylformamideHCID 6228—
ProductHCID 91513383HCID 9151338372.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of sodium hydride (71 mg, 1.8 mmol) in dry DMF (5 mL) was cooled to 0° C., and a solution of methyl 2-azido-4-O-benzyl-2-deoxy-3-O-(4-methoxybenzyl)-1-thio-β-D-glucopyranoside (33) (680 mg, 1.5 mmol) in dry DMF (5 mL) was added dropwise in 30 minutes. The resulting solution was stirred at room temperature for 30 minutes and 4-chlorobenzyl chloride (295 mg, 1.5 mmol) was added dropwise at 0° C. The reaction mixture was stirred at room temperature for 4.5 hours, cooled at 0° C. and dry methanol (1 mL) was added dropwise. The reaction mixture was concentrated under reduced pressure, then xylene (10 mL) was co-evaporated from the residue. The residue was treated with hexane (10 mL) and filtered to give methyl 2-azido-4-O-benzyl-6-O-(4-chlorobenzyl)-2-deoxy-3-O-(4-methoxybenzyl)-1-thio-β-D-glucopyranoside (34) (620 mg, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953850B1
Source datasetuspto-grants-2005_10
ORD IDord-adadd1e99787477d8667c5cafee65025
Source noteuspto-grants-2005_10